TYR, tyrosinase, 7299

N. diseases: 281; N. variants: 121
Disease: Skin Pigmentation ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		0.100 GeneticVariation phenotype GWASCAT Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. 30166351 2018
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		0.100 GeneticVariation phenotype GWASCAT A genomewide association study of skin pigmentation in a South Asian population. 17999355 2007
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation 		0.100 GeneticVariation phenotype GWASDB A genomewide association study of skin pigmentation in a South Asian population. 17999355 2007